20-Hz operation of an eye-safe cascade Raman laser with a Ba(NO3)2 crystal

Operation of a 1.598-μm eye-safe third-Stokes Raman laser with a Ba(NO₃)₂ crystal pumped by a 1.064-μm Nd:YAG laser is described. We observed a substantial decrease in the output energy during the first 50 s of the continuous operation at 20 Hz. The energy drop is ∼76% of the initial third-Stokes output. We confirmed negative thermal lensing and thermally induced birefringence in the crystal. With a concave cavity mirror at a matched curvature to the thermal lensing, we obtained an output energy of 11 mJ at 20 Hz. TEM₀₀ output was also obtained with a smaller pump-beam diameter with a highest conversion efficiency of 15.5% for a pumping power of only 45 MW/cm² (0.9 J/cm²). Received: 20 November 2001 / Revised version: 20 February 2002 / Published online: 2 May 2002     

Simultaneous generation of a proton beam and terahertz radiation in high-intensity laser and thin-foil interaction

We have observed simultaneously both the fast proton generation and terahertz (THz) radiation in the laser pulse interaction with a 5-μm thick titanium target. In order to control the proton acceleration and THz radiation, we have changed the duration of the amplified spontaneous emission (ASE) preceding the main pulse generated by the high-intensity Ti:sapphire laser. A fast proton beam with the maximal energy of ∼ 490 keV has been realized by reducing the duration of the ASE. Simultaneously, an intense emission of THz radiation is observed for various ASE durations. We propose the antenna mechanism for the THz radiation, according to which the fast electrons moving along the target surface emit the low-frequency electromagnetic wave. PACS 52.25.Os; 52.38.Kd; 52.50.Jm     

Germania/ormosil hybrid materials derived at low temperature for photonic applications

We report on germania/organically modified silane (ormosil) hybrid materials produced by the sol–gel technique for photonic applications. Acid-catalyzed solutions of γ-glycidoxypropyltrimethoxysilane mixed with germanium isopropoxide have been used as precursors for the hybrid materials. Planar waveguide films with a thickness of about 2 μm have been prepared by a single spin-coating process and low-temperature heat treatment from these high germanium content hybrid materials. Atomic force microscopy, thermal gravimetric analysis, UV–visible spectroscopy, and Fourier-transform infrared spectroscopy have been used to investigate the optical and structural properties of the films. The results have indicated that a dense, low absorption, and high transparency (in the visible range) waveguide film could be achieved at a low temperature. A strong UV-absorption region at short wavelengths ∼200 nm, accompanied by a shoulder peaked at ∼240 nm, has been noticed due to the neutral oxygen monovacancy defects. The propagation mode and loss properties of the planar waveguide films have also been investigated by using a prism-coupling technique. Received: 5 November 2002 / Revised version: 27 December 2002 / Published online: 19 March 2003 RID="*" ID="*"Corresponding author. Fax: +65-67909081, E-mail: ewxque@ntu.edu.sg     

Efficient J=0-1 soft-X-ray lasing in neon-like ions at pump powers below 250 GW

2 . By using a 0.7% prepulse that precedes the main pulse by 5 ns and applying a total pump energy of 100 J or less, the J=0-1 lasing is at least one order of magnitude higher than the non-lasing background. For the 32.6-nm line of Ti, the 25.5-nm line of Fe, and the 23.1-nm line of Ni, gain coefficients of (±) 4.20.4cm^-1, (±) 3.90.3cm^-1, and (±) 3.60.6cm^-1, respectively, were measured for 2.4-cm-long curved targets, resulting in gain–length products of ∼10. Angle-resolved spectra indicate a beam divergence of 3 mrad (FWHM), typically. The space-resolved spectra show that the J=0-1 lasing lines are emitted from an approximately 60-μm-wide (FWHM) plasma region, whereas the nearby continuum emission is produced in a considerably broader plasma region of ∼250 μm. Lasing at 25.5 nm in neon-like iron was observed at a pump power as low as 180 GW (∼9 TW/cm²), with, however, considerable shot-to-shot scatter in the absolute laser output. Received: 5 September 1997/Revised version: 10 November 1997     

Continuous-wave tunable Cr2+:ZnS laser

We report the first continuous-wave tunable over ∼280 nm around 2.3 μm room-temperature operation of a chemical vapor transport-grown and diffusion-doped Cr²⁺:ZnS laser, pumped by a Co:MgF₂ laser at 1.67 μm and generating over 100 mW of output power at 16% slope efficiency. The self-consistent results of the laser and spectroscopic analysis demonstrate a large potential of this crystal as an active medium for diode-pumped tunable mid-infrared sources. Received: 7 January 2002 / Revised: 14 March 2002 / Published online: 2 May 2002     

Temperature-tuned difference-frequency mixing in periodically poled KTiOPO4

4 (PPKTP). We generated 12 μW of radiation tunable around 1.6 μm by difference-frequency mixing of the outputs of a frequency-doubled Nd:YLF laser at 523 nm (240 mW) and a tunable Ti:sapphire laser near 760 nm (340 mW). A temperature tuning rate of 0.73 nm/°C for the generated wavelength and a FWHM temperature acceptance bandwidth of 6.9 °C cm was observed. The effective d₃₃ coefficient was estimated to be ∼5 pm/V. Received: 02 September 1998     

Bragg reflection waveguide: Anti-mirror reflection and light slowdown

The effect of the light group velocity reduction in dielectric Bragg reflection waveguide structures (SiO₂/TiO₂) in the vicinity of the cutoff frequency is studied experimentally. The effect of anti-mirror reflection specific to Bragg reflection waveguides is described and employed to detect slow light. Experiments were performed using Ti:sapphire laser pulses ∼100 fs in length. The group index n _g ∼ 30 with a fractional pulse delay (normalized to the pulse width) of ∼10 is demonstrated. The problems and prospects of the implementation of slow-light devices based on Bragg reflection waveguide structures are discussed.     

Photoacoustic gas sensing employing fundamental and frequency-doubled radiation of a continuously tunable high-pressure CO2 laser

We present the first photoacoustic spectrometer for gas sensing employing both the fundamental and the frequency-doubled radiation of a continuously tunable high-pressure CO₂ laser with room temperature operation. A quasi-phase-matched diffusion-bonded GaAs crystal is used in the system for second-harmonic generation. A pulsed photoacoustic detection scheme with a non-resonant cell, equipped with an 80-microphone array, is employed. The wide continuous tuning range in the fundamental (9.2–10.7 μm) and the frequency-doubled (4.6–5.35 μm) regimes, together with the narrow linewidth of 540 MHz (0.018 cm^-1) for the 10-μm region and of 1050 MHz (0.0315 cm^-1) for the 5-μm region, allow the measurement of gas mixtures, individual species and isotope discrimination. This is illustrated with measurements on NO and CO₂. The measured isotope ratio ¹⁵ NO/¹⁴ NO=(3.58±0.55)×10^-3 agrees well with the literature (3.700×10^-3) and demonstrates the good selectivity of the system. Received: 30 April 2002 / Revised version: 10 June 2002 / Published online: 2 September 2002 RID="*" ID="*"Corresponding author. Fax: +41-1/633-1077, E-mail: sigrist@iqe.phys.ethz.ch     

Multi-layer cladding leaky planar waveguide for high-power applications

We design a multi-layer cladding large-core planar waveguide that supports a single guided mode. The waveguide works on the principle of higher-order mode discrimination. The cladding of the waveguide is formed by alternate low- and high- index regions, which helps leaking out of higher-order modes while retaining the fundamental mode over the entire length of the waveguide. The structure is analyzed by the transfer-matrix method and the leakage losses of the modes have been calculated. We show that a waveguide formed in silica with numerical aperture 0.24 and core width 10 μm can be designed to exhibit single-mode operation at 1550-nm wavelength. Such a structure should find applications in high-power planar waveguide lasers and amplifiers.     

Structure,transport and field-emission properties of compound nanotubes: CN<Subscript>x</Subscript> vs. BNC<Subscript>x</Subscript> (<Emphasis Type="Italic">x</Emphasis><0.1)

Transport and field-emission properties of as-synthesized CN_x and BNC_x (x<0.1) multi-walled nanotubes were compared in detail. Individual ropes made of these nanotubes and macrofilms of those were tested. Before measurements, the nanotubes were thoroughly characterized using high-resolution and energy-filtered electron microscopy, electron diffraction and electron-energy-loss spectroscopy. Individual ropes composed of dozens of CN_x nanotubes displayed well-defined metallic behavior and low resistivities of ∼10–100 kΩ or less at room temperature, whereas those made of BNC_x nanotubes exhibited semiconducting properties and high resistivities of ∼50–300 MΩ. Both types of ropes revealed good field-emission properties with emitting currents per rope reaching ∼4 μA(CN_x) and ∼2 μA (BNC_x), albeit the latter ropes se- verely deteriorated during the field emission. Macrofilms made of randomly oriented CN_x or BNC_x nanotubes displayed low and similar turn-on fields of ∼2–3 V/μm. 3 mA/cm² (BNC_x) and 5.5 mA/cm² (CN_x) current densities were reached at 5.5 V/μm macroscopic fields. At a current density of 0.2–0.4 mA/cm² both types of compound nanotubes exhibited equally good emission stability over tens of minutes; by contrast, on increasing the current density to 0.2–0.4 A/cm², only CN_x films continued to emit steadily, while the field emission from BNC_x nanotube films was prone to fast degradation within several tens of seconds, likely due to arcing and/or resistive heating. Received: 29 October 2002 / Accepted: 1 November 2002 / Published online: 10 March 2003 RID="*" ID="*"Corresponding author. Fax: +81-298/51-6280, E-mail: golberg.dmitri@nims.go.jp     

1.53 μm photoluminescence from ErYb(DBM)<Subscript>3</Subscript>MA containing polymer

We investigated the optical properties of the ErYb(DBM)₃MA complexes and the ErYb(DBM)₃MA containing polymer. Absorption and photoluminescence spectra confirm that the presence of Yb³⁺ ions enhances luminescence efficiency of Er³⁺ ions. The full width at half maximum bandwidth (FWHM) is ∼80 nm wide around 1.53 μm wavelength. We also fabricated ErYb containing polymeric channel waveguides using reactive ion etching technique. As an input pump of 120 mW was used, a ∼1.53 μm spontaneous emission was obtained in a 4-mm-long waveguide. PACS 42.00.00; 42.70.Jk; 42.82.Et     

A UV–Visible–NIR fluorescence lifetime imaging microscope for laser-based biological sensing with picosecond resolution

This article describes the design and characterization of a wide-field, time-domain fluorescence lifetime imaging microscopy (FLIM) system developed for picosecond time-resolved biological imaging. The system consists of a nitrogen-pumped dye laser for UV–visible–NIR excitation (337.1–960 nm), an epi-illuminated microscope with UV compatible optics, and a time-gated intensified CCD camera with an adjustable gate width (200 ps-10^-3 s) for temporally resolved, single-photon detection of fluorescence decays with 9.6-bit intensity resolution and 1.4-μm spatial resolution. Intensity measurements used for fluorescence decay calculations are reproducible to within 2%, achieved by synchronizing the ICCD gate delay to the excitation laser pulse via a constant fraction optical discriminator and picosecond delay card. A self-consistent FLIM system response model is presented, allowing for fluorescence lifetimes (0.6 ns) significantly smaller than the FLIM system response (1.14 ns) to be determined to 3% of independently determined values. The FLIM system was able to discriminate fluorescence lifetime differences of at least 50 ps. The spectral tunability and large temporal dynamic range of the system are demonstrated by imaging in living human cells: UV-excited endogenous fluorescence from metabolic cofactors (lifetime ∼1.4 ns); and 460-nm excited fluorescence from an exogenous oxygen-quenched ruthenium dye (lifetime ∼400 ns). Received: 23 February 2003 / Published online: 22 May 2003 RID="*" ID="*"Corresponding author. Fax: +1-734/9361-905, E-mail: mycek@umich.edu     

Synchronously pumped femtosecond optical parametric oscillator based on AgGaSe2 tunable from 2 μm to 8 μm

The operation of a continuous-wave mode-locked silver gallium selenide (AgGaSe₂) optical parametric oscillator (OPO) is reported. The OPO was synchronously excited by 120-fs-long pulses of 1.55-μm radiation at a repetition rate of 82 MHz. The 1.55-μm radiation is generated by a noncritically phasematched cesium-titanyl-arsenate (CTA)-OPO pumped by a mode-locked Ti:sapphire laser. The AgGaSe₂-OPO generates signal and idler radiation in the range from 1.93 μm to 2.49 μm and from 4.1 μm to 7.9 μm, respectively. Up to 67 mW of signal wave output power has been obtained. The experimentally determined pulse duration and chirp parameters are in reasonable agreement with results from a numerical model taking into account group velocity mismatch, group velocity dispersion, self phase modulation, and chirp enhancement. Received: 6 August 1999 / Revised version: 4 October 1999 / Published online: 3 November 1999     

Low-threshold mid-infrared optical parametric oscillation in periodically poled LiNbO3 synchronously pumped by a Ti:sapphire laser

We report the generation of tunable high-repetition-rate optical pulses in the mid-infrared using synchronously pumped parametric oscillation in periodically poled LiNbO₃ (PPLN). Using a Kerr-lens-mode-locked Ti:sapphire laser as the pump source and a PPLN crystal incorporating grating periods of 21.0–22.4 μm, we have achieved wavelength conversion in the -–4 6μm spectral range in the mid-infrared. The use of a semi-monolithic cavity design and hemispherical focusing has permitted pulse generation in the strong idler absorption region of PPLN, resulting in a simple, compact, all-solid-state configuration with a pump power threshold as low as 17 mW and mid-infrared idler powers of up to 64 mW at 9% extraction efficiency. Signal output powers of up to 280 mW at 35% extraction efficiency are available over the -–1.004 1.140μm spectral range at 80.5 MHz and pulse repetition rates at harmonics of the fundamental frequency up to 322 MHz have also been obtained. Received: 5 December 2000 / Revised version: 23 January 2001 / Published online: 27 April 2001     

Field emission from single-walled carbon nanotubes aligned on a gold plate using a self-assembly monolayer

Field emission from single-walled carbon nanotubes (SWNTs) aligned on a patterned gold surface is reported. The SWNT emitters were prepared at room temperature by a self-assembly monolayer technique. SWNTs were cut into sub-micron lengths by sonication in an acidic solution. Cut SWNTs were attached to the gold surface by the reaction between the thiol groups and the gold surface. The field-emission measurements showed that the turn-on field was 4.8 V/μm at an emission current density of 10 μA/cm². The current density was 0.5 mA/cm² at 6.6 V/μm. This approach provides a novel route for fabricating CNT-based field-emission displays. Received: 3 May 2002 / Accepted: 6 May 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +82-54/279-8298, E-mail: ce20047@postech.ac.kr     

Broadband single-transverse-mode fluorescence sources based on ribs fabricated in pulsed laser deposited Ti:sapphire waveguides

Active rib waveguides with depths and widths varying from 3 to 5 m and from 9 to 24 m, respectively, have been structured by Ar⁺-beam etching in pulsed laser deposited Ti:sapphire layers. Losses in the channel structures were essentially at the same levels as the unstructured planar waveguide host, therefore suggesting that there is no significant additional contribution to loss from the rib-fabrication procedure. Measurements of the beam-propagation factors, M_x² and M_y², indicate single-transverse-mode fluorescence emission. The fluorescence output power was in the order of 300 W when the structures were pumped by a 3-W multiline argon laser. These characteristics make the rib structures suitable as light sources for optical coherence tomography applications and facilitate their coupling to the optical fibre interferometers of such systems. PACS 42.70.Hj; 42.82.Et; 42.79.Gn; 81.15.Fg; 42.30.Wb     

Synthesis of LaB6 micro/nano structures using picosecond (Nd:YAG) laser and its field emission investigations

Micro/nano structures have been obtained by laser surface treatment on sintered LaB₆ pellets employing a picosecond pulsed Nd:YAG laser at a pressure of ∼1×10⁻³ mbar. The X-ray diffraction pattern of the laser treated pellet shows a set of well defined diffraction peaks, indexed to the cubic phase of LaB₆ only. The scanning electron microscope studies reveal formation of micro and nano structures upon laser treatment and the resultant surface morphology is found to be strongly influenced by the laser fluence. Field electron emission studies made on the LaB₆ pellet, treated with optimized laser fluence, have been performed in a planar diode configuration under ultra high vacuum conditions. The threshold field required to draw an emission current density of ∼10 μA/cm² has been found to be ∼2.3 V/μm and a current density of ∼530 μA/cm² has been drawn at an applied field of 5.2 V/μm. The Fowler-Nordheim plot is found to be linear in accordance with the quantum mechanical tunneling phenomenon, confirming the metallic nature of the emitter. The emission current at the pre-set value ∼10 μA shows very good stability over a period of more than 3 hours. The present results emphasize the effectiveness of a picosecond laser treatment towards fabrication of a nano metric LaB₆ emitter for high current density applications.     

Epitaxial growth and spectroscopic investigation of BaSO4:Mn6+ layers

We report on the first layer growth of a Mn⁶⁺-doped material. Large-size BaSO₄ substrates of 10×6×4 mm³ were grown from a LiCl solvent by the flux method. Flat surfaces of undoped BaSO₄ were then achieved by use of liquid-phase epitaxy (LPE) from a CsCl–KCl–NaCl solvent. Finally, BaSO₄:Mn⁶⁺ layers were grown by LPE with growth velocities of approximately 3 μm h^-1, at temperatures of 550–508 °C. Absorption, luminescence, luminescence-excitation and luminescence-decay measurements confirmed the incorporation of manganese solely in its hexavalent oxidation state. This material possesses potential as a near-infrared tunable laser with a wavelength range larger than Ti:sapphire. Received: 7 January 2002 / Revised version: 30 March 2002 / Published online: 8 August 2002     

New photopolymerizable holographic recording material based on polyvinylalcohol and 2-hydroxiethylmethacrylate (HEMA)

We have developed a new polyvinylalcohol-based photopolymeric holographic recording material. The recording is obtained by the copolymerization of acrylamide and 2-hydroxiethylmethacrylate (HEMA). Diffraction efficiencies near 70% are obtained with exposures of ≈65 mJ/cm² in materials of 110-μm thickness. The addition of HEMA increases the thickness of the film, which results in improved storage capacity for holographic optical storage. Received: 7 March 2002 / Published online: 2 May 2002